ClearanceBrief
510(k) K925992 ยท KMK Device, Intravascular Catheter Securement

DUODERM TRANSPARENT HYDROCOLLOID DRESSING

ApplicantConvatec, A Division of E.R. Squibb & Sons, Princeton NJ, US
DecisionSubstantially Equivalent, Oct 15, 1993
ReceivedNov 25, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925992

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.